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124337-86-6

Δ1.6-1-triemthylsilyloxy-3-methyl-3-vinylcyclohexene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124337-86-6 Structure

  • Basic information

    1. Product Name: Δ1.6-1-triemthylsilyloxy-3-methyl-3-vinylcyclohexene
    2. Synonyms: Δ1.6-1-triemthylsilyloxy-3-methyl-3-vinylcyclohexene
    3. CAS NO:124337-86-6
    4. Molecular Formula:
    5. Molecular Weight: 210.392
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124337-86-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Δ1.6-1-triemthylsilyloxy-3-methyl-3-vinylcyclohexene(CAS DataBase Reference)
    10. NIST Chemistry Reference: Δ1.6-1-triemthylsilyloxy-3-methyl-3-vinylcyclohexene(124337-86-6)
    11. EPA Substance Registry System: Δ1.6-1-triemthylsilyloxy-3-methyl-3-vinylcyclohexene(124337-86-6)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 124337-86-6(Hazardous Substances Data)

124337-86-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124337-86-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,3,3 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 124337-86:
(8*1)+(7*2)+(6*4)+(5*3)+(4*3)+(3*7)+(2*8)+(1*6)=116
116 % 10 = 6
So 124337-86-6 is a valid CAS Registry Number.

124337-86-6Relevant articles and documents

TOTAL SYNTHESIS OF MARINE ALKALOIDS (+/-)-HAPALINDOLES J AND M

Muratake, Hideaki,Natsume, Mitsutaka

, p. 1815 - 1818 (1989)

Marine alkaloids hapalindoles J 1 and M 2 were concisely synthesized in the racemic form from a tertiary alcohol 4 by way of 7, 9, 11, and 17, using unusual LiAlH4 reduction of 11 as a key reaction step.

SYNTHETIC STUDIES OF MARINE ALKALOIDS HAPALINDOLES. Part 1. TOTAL SYNTHESIS OF (+/-)-HAPALINDOLES J and M

Muratake, Hideaki,Natsume, Mitsutaka

, p. 6331 - 6342 (2007/10/02)

The first concise synthesis of marine indole alkaloids (+/-) hapalindoles J (4) and M (5) was achieved in seven or six steps starting from a readily available compound 6 using important key reactions, 6 -> 7 -> 8 and 35 -> 41 or 5.

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